| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004610 |
BXGD000281 |
Bacteremia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0006287 |
BXGD000390 |
Bronchopulmonary Dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0009319 |
BXGD000596 |
Colitis |
Digestive System Diseases |
| C0009324 |
BXGD000597 |
Ulcerative Colitis |
Digestive System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009404 |
BXGD000606 |
Colorectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0010346 |
BXGD000664 |
Crohn Disease |
Digestive System Diseases |
| C0010674 |
BXGD000683 |
Cystic Fibrosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases |
| C0011175 |
BXGD000701 |
Dehydration |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0011853 |
BXGD000752 |
Diabetes Mellitus, Experimental |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011991 |
BXGD000766 |
Diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0013369 |
BXGD000821 |
Dysentery |
Digestive System Diseases |
| C0017152 |
BXGD001096 |
Gastritis |
Digestive System Diseases |
| C0017572 |
BXGD001121 |
Gingival Recession |
Stomatognathic Diseases |
| C0020443 |
BXGD001385 |
Hypercholesterolemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0021831 |
BXGD001516 |
Intestinal Diseases |
Digestive System Diseases |
| C0022104 |
BXGD001529 |
Irritable Bowel Syndrome |
Digestive System Diseases |
| C0022951 |
BXGD001595 |
Lactose Intolerance |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0023493 |
BXGD001672 |
Adult T-Cell Lymphoma/Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023508 |
BXGD001675 |
White Blood Cell Count procedure |
|
| C0023601 |
BXGD001687 |
Leydig Cell Tumor |
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases |
| C0024131 |
BXGD001736 |
Lupus Vulgaris |
Infections; Skin and Connective Tissue Diseases |
| C0024138 |
BXGD001738 |
Lupus Erythematosus, Discoid |
Skin and Connective Tissue Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024523 |
BXGD001781 |
Malabsorption Syndrome |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0028768 |
BXGD002084 |
Obsessive-Compulsive Disorder |
Mental Disorders |
| C0028960 |
BXGD002101 |
Oligospermia |
Male Urogenital Diseases |
| C0029443 |
BXGD002152 |
Osteomyelitis |
Infections; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0032285 |
BXGD002344 |
Pneumonia |
Infections; Respiratory Tract Diseases |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032580 |
BXGD002362 |
Adenomatous Polyposis Coli |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0035222 |
BXGD002513 |
Respiratory Distress Syndrome, Adult |
Respiratory Tract Diseases |
| C0035319 |
BXGD002534 |
Retinal Necrosis Syndrome, Acute |
Eye Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0037278 |
BXGD002678 |
Skin Diseases, Infectious |
Infections; Skin and Connective Tissue Diseases |
| C0038166 |
BXGD002736 |
Staphylococcal Skin Infections |
Infections; Skin and Connective Tissue Diseases |
| C0039590 |
BXGD002822 |
Testicular Neoplasms |
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases |
| C0040517 |
BXGD002872 |
Gilles de la Tourette syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0085207 |
BXGD003140 |
Gestational Diabetes |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085278 |
BXGD003150 |
Antiphospholipid Syndrome |
Immune System Diseases |
| C0085409 |
BXGD003168 |
Polyendocrinopathies, Autoimmune |
Immune System Diseases; Endocrine System Diseases |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0155707 |
BXGD003813 |
Trifascicular block |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0162429 |
BXGD003942 |
Malnutrition |
Nutritional and Metabolic Diseases |
| C0220620 |
BXGD004299 |
Gastrointestinal Carcinoid Tumor |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0220981 |
BXGD004348 |
Metabolic acidosis |
Nutritional and Metabolic Diseases |
| C0264913 |
BXGD005436 |
Left posterior fascicular block |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0266815 |
BXGD005717 |
Cow milk allergy |
Digestive System Diseases; Immune System Diseases |
| C0268179 |
BXGD005846 |
Lactase Deficiency, Congenital |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0268181 |
BXGD005847 |
Lactose Intolerance, Adult Type |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0272051 |
BXGD006298 |
Xerocytosis |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0272322 |
BXGD006343 |
Severe hereditary factor VIII deficiency disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0272375 |
BXGD006359 |
Antithrombin III Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0279980 |
BXGD006701 |
Extra-osseous Ewing's sarcoma |
Neoplasms |
| C0311370 |
BXGD006882 |
Lupus anticoagulant disorder |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0333047 |
BXGD006919 |
Recession |
|
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0341106 |
BXGD007389 |
Eosinophilic esophagitis |
Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0403823 |
BXGD008315 |
Asthenozoospermia |
Male Urogenital Diseases |
| C0403824 |
BXGD008316 |
Teratozoospermia |
Male Urogenital Diseases |
| C0409974 |
BXGD008401 |
Lupus Erythematosus |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases |
| C0432306 |
BXGD008770 |
Ichthyosis Bullosa of Siemens |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0521170 |
BXGD009131 |
Osteoporotic Fractures |
Wounds and Injuries |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0578159 |
BXGD009543 |
Antibiotic-associated diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1844680 |
BXGD014661 |
DEAFNESS-HYPOGONADISM SYNDROME |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases |
| C1847501 |
BXGD014866 |
Glut1 Deficiency Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1851841 |
BXGD015242 |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases |
| C1853193 |
BXGD015312 |
Recurrent skin infections |
Infections; Skin and Connective Tissue Diseases |
| C1857231 |
BXGD015685 |
LACTASE PERSISTENCE |
|
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C2751492 |
BXGD017718 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C2985280 |
BXGD018223 |
Blood Protein Measurement |
|
| C3541994 |
BXGD019100 |
Drug Hypersensitivity Syndrome |
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders |
| C4302261 |
BXGD022535 |
Primary lactase deficiency |
|
| C4476604 |
BXGD022839 |
Decreased small intestinal mucosa lactase activity |
|
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|